US6372821B1 - Low VOC (volatile organic compounds), dimethyl-2-piperidone solvent-based, PVC and CPVC pipe and component adhesives and primers containing minimal or no tetrahydrofuran - Google Patents
Low VOC (volatile organic compounds), dimethyl-2-piperidone solvent-based, PVC and CPVC pipe and component adhesives and primers containing minimal or no tetrahydrofuran Download PDFInfo
- Publication number
- US6372821B1 US6372821B1 US09/651,824 US65182400A US6372821B1 US 6372821 B1 US6372821 B1 US 6372821B1 US 65182400 A US65182400 A US 65182400A US 6372821 B1 US6372821 B1 US 6372821B1
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- United States
- Prior art keywords
- ketone
- adhesive
- pvc
- methyl
- cpvc
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- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 132
- 239000000853 adhesive Substances 0.000 title claims abstract description 131
- 229920000915 polyvinyl chloride Polymers 0.000 title claims abstract description 107
- 239000004800 polyvinyl chloride Substances 0.000 title claims abstract description 107
- 239000004801 Chlorinated PVC Substances 0.000 title claims abstract description 76
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 title claims abstract description 75
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 title claims abstract description 51
- RJLKIAGOYBARJG-UHFFFAOYSA-N 1,3-dimethylpiperidin-2-one Chemical compound CC1CCCN(C)C1=O RJLKIAGOYBARJG-UHFFFAOYSA-N 0.000 title claims abstract description 18
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 title claims description 25
- 239000002904 solvent Substances 0.000 title abstract description 45
- 239000012855 volatile organic compound Substances 0.000 title description 33
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims abstract description 123
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims abstract description 103
- 239000011347 resin Substances 0.000 claims abstract description 89
- 229920005989 resin Polymers 0.000 claims abstract description 89
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims abstract description 66
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 claims abstract description 52
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 claims abstract description 50
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 14
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 claims abstract description 12
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229940043265 methyl isobutyl ketone Drugs 0.000 claims abstract description 12
- 238000009835 boiling Methods 0.000 claims description 60
- 150000002576 ketones Chemical class 0.000 claims description 56
- 239000004925 Acrylic resin Substances 0.000 claims description 18
- 229920000178 Acrylic resin Polymers 0.000 claims description 18
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N 3-Methylbutan-2-one Chemical compound CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 claims description 12
- FFWSICBKRCICMR-UHFFFAOYSA-N 5-methyl-2-hexanone Chemical compound CC(C)CCC(C)=O FFWSICBKRCICMR-UHFFFAOYSA-N 0.000 claims description 10
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims description 10
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 8
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 claims description 7
- 229920001519 homopolymer Polymers 0.000 claims description 6
- 239000013008 thixotropic agent Substances 0.000 claims description 6
- RHLVCLIPMVJYKS-UHFFFAOYSA-N 3-octanone Chemical compound CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 5
- 239000000945 filler Substances 0.000 claims description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 4
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 3
- 238000005660 chlorination reaction Methods 0.000 claims description 3
- 229910021485 fumed silica Inorganic materials 0.000 claims description 3
- 229920001897 terpolymer Polymers 0.000 claims description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- 239000000440 bentonite Substances 0.000 claims description 2
- 229910000278 bentonite Inorganic materials 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 239000000919 ceramic Substances 0.000 claims description 2
- 239000004927 clay Substances 0.000 claims description 2
- 229910002026 crystalline silica Inorganic materials 0.000 claims description 2
- 239000000155 melt Substances 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- 235000012239 silicon dioxide Nutrition 0.000 claims description 2
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 claims 2
- QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 claims 1
- 150000004684 trihydrates Chemical class 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 61
- 229920001169 thermoplastic Polymers 0.000 abstract description 11
- 239000004416 thermosoftening plastic Substances 0.000 abstract description 11
- 150000001875 compounds Chemical class 0.000 abstract description 6
- 229910002016 AerosilĀ® 200 Inorganic materials 0.000 abstract description 4
- -1 specifically Substances 0.000 abstract description 4
- 150000004292 cyclic ethers Chemical class 0.000 abstract description 3
- 239000003085 diluting agent Substances 0.000 abstract description 3
- 238000003466 welding Methods 0.000 abstract description 3
- 238000009472 formulation Methods 0.000 description 14
- 239000004568 cement Substances 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 230000002706 hydrostatic effect Effects 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 238000000518 rheometry Methods 0.000 description 5
- 239000003381 stabilizer Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000002318 adhesion promoter Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- WWNGFHNQODFIEX-UHFFFAOYSA-N buta-1,3-diene;methyl 2-methylprop-2-enoate;styrene Chemical compound C=CC=C.COC(=O)C(C)=C.C=CC1=CC=CC=C1 WWNGFHNQODFIEX-UHFFFAOYSA-N 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- YXHVIDNQBMVYHQ-UHFFFAOYSA-N 1,5-dimethylpiperidin-2-one Chemical compound CC1CCC(=O)N(C)C1 YXHVIDNQBMVYHQ-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 2
- 229920009204 Methacrylate-butadiene-styrene Polymers 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 235000012206 bottled water Nutrition 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 239000003651 drinking water Substances 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- WSGCRAOTEDLMFQ-UHFFFAOYSA-N nonan-5-one Chemical compound CCCCC(=O)CCCC WSGCRAOTEDLMFQ-UHFFFAOYSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- JBCMUNOVVMEKMO-UHFFFAOYSA-N 1,4-dimethylpiperidin-2-one Chemical compound CC1CCN(C)C(=O)C1 JBCMUNOVVMEKMO-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 206010007269 Carcinogenicity Diseases 0.000 description 1
- 229920005479 LuciteĀ® Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- RREGISFBPQOLTM-UHFFFAOYSA-N alumane;trihydrate Chemical compound O.O.O.[AlH3] RREGISFBPQOLTM-UHFFFAOYSA-N 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000008365 aromatic ketones Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000007670 carcinogenicity Effects 0.000 description 1
- 231100000260 carcinogenicity Toxicity 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000011499 joint compound Substances 0.000 description 1
- 238000007726 management method Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000001062 red colorant Substances 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000013024 troubleshooting Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000001060 yellow colorant Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/12—Bonding of a preformed macromolecular material to the same or other solid material such as metal, glass, leather, e.g. using adhesives
- C08J5/124—Bonding of a preformed macromolecular material to the same or other solid material such as metal, glass, leather, e.g. using adhesives using adhesives based on a macromolecular component
- C08J5/125—Adhesives in organic diluents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/07—Aldehydes; Ketones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J127/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Adhesives based on derivatives of such polymers
- C09J127/02—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J127/04—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Adhesives based on derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C09J127/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J127/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Adhesives based on derivatives of such polymers
- C09J127/22—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Adhesives based on derivatives of such polymers modified by chemical after-treatment
- C09J127/24—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Adhesives based on derivatives of such polymers modified by chemical after-treatment halogenated
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00Ā -Ā C08L49/00, or C08L55/00Ā -Ā C08L57/00; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
- C08L33/12—Homopolymers or copolymers of methyl methacrylate
Definitions
- the present invention relates generally to thermoplastic pipe adhesive and primer compositions, and, more particularly, to adhesives and primers used for joining PCV (polyvinyl chloride) and CPVC (chlorinated PVC) pipe.
- PCV polyvinyl chloride
- CPVC chlorinated PVC
- the PVC and CPVC pipe adhesives and primers disclosed and claimed herein are solvent-based, having an environmentally-acceptable VOC (volatile organic compounds) content.
- Solvent-based adhesives or cements
- solvent-based adhesives have been in use for joining thermoplastic pipe for over 30 years.
- the development of these adhesives is largely responsible for growth of the thermoplastic pipe industry.
- Several billion pounds of plastic pipe are produced each year in North America. Rapid-setting, solvent-based adhesives weld the pipes together in a timely manner.
- These rapid-setting adhesives allow for the testing and trouble-shooting of piping systems in a matter of hours while maintaining the long-term durability of the pipe itself.
- solvent-based adhesives have made the joining of plastic pipe by solvent-based adhesives a practical and economic system.
- the solvent-based adhesives work primarily by two means of action. First, the solvent portion of the formulation softens the outer surfaces of the pipe through solvation of the plastic. Subsequently, the adhesive joint ācuresā (hardens) by means of the solvents evaporating to the surrounding atmosphere from the pipe. Secondly, the resin dissolved in the adhesive dries through solvent evaporation and provides continuity between the welded pipe surfaces which aid in preserving the integrity of the entire pipe system.
- thermoplastic piping systems are constructed each day throughout the world, primarily by the means previously described. These systems are used in the transfer of potable water for drinking; residential hot and cold water systems; drain, waste, and vent (DWV) applications in home and industry; turf and agricultural sprinkler systems; jacuzzi, spa and tub connections, residential and commercial fire sprinkler systems; etc. These systems are crucial to the maintenance of safe and healthy means of transport of water and other chemicals throughout the world.
- DWV drain, waste, and vent
- Typical solids (non-volatile) contents of plastic pipe adhesives are 10 to 20% for both PVC and CPVC.
- the balance of the formulation is solvent.
- the solvents normally used e.g., tetrahydrofuran (THF), methyl ethyl ketone (MEK), and acetone are considered to be VOCs. That is, they are volatile compounds which contain the element carbon excluding methane, carbon monoxide, carbon dioxide, carbonic acid, metallic carbides and carbonates, ammonium carbonate, and exempt compounds, such as methylene chloride and 1,1,1-trichlorethane.
- solvents such as cyclohexanone and dimethyl formamide (in the case of PVC) and cyclohexanone (in the case of CPVC)
- the amount of such solvents are typically minor, considerably less than 15 wt % (in the case of PVC) and 10 wt % (in the case of CPVC) of the total adhesive concentration.
- Typical VOC values of present commercial PVC solvent adhesives range from 750 to 850 grams/liter and for CPVC solvent adhesives range from 775 to 850 g/l.
- SCAQMD South Coast Air Quality Management District
- SCAQMD Rule 1168 specifies a VOC level for PVC adhesives of 510 g/l or less and for CPVC adhesives of 490 g/l or less, as determined by Method 316-A. All PVC and CPVC adhesives used after Jan. 24, 1994, are required to meet that maximum allowed level.
- THF tetrahydrofuran
- PVC and CPVC adhesive compositions typically, 25 to 75 wt %
- THF is under extensive investigation, both with regard to worker health (exposure during pipe assembly) and potable water issues.
- THF is a high vapor pressure, fast-evaporating solvent that heavily contributes to the VOC level. It is highly desirable to reduce THF levels, but still maintain the adhesive-contributing properties that THF offers, i.e., fast-setting, durable pipe joints.
- NMP N-methyl pyrrolidone
- thermoplastic pipe adhesives are formulated with large amounts of low vapor pressure solvents blends, such as di-methyladipate (available from E. I. DuPont de Nemours as DBE-6) and NMP and/or alkyl-substituted naphthalene (U.S. Pat. No. 5,821,289, issued to C. D. Congelio et al) to reduce VOC levels, but generally these type of adhesives require longer set times before water pressure testing of the system can be made. Also, these slower setting adhesives are less effective in colder environments.
- di-methyladipate available from E. I. DuPont de Nemours as DBE-6
- NMP and/or alkyl-substituted naphthalene U.S. Pat. No. 5,821,289, issued to C. D. Congelio et al
- Still another method to formulate low VOC cements for thermoplastic pipe and other PVC and CPVC extruded articles is to incorporate higher amounts of resin(s). This does indeed reduces VOC levels, but is less cost effective and generally slower than cements containing lower weight percent of resin.
- novel low VOC solvent-based adhesives comprising a mixture of low vapor pressure isomeric dimethyl-2-piperidones (DMPD) blended with (1) a non-solvent diluent, specifically, acetone (a VOC-exempt compound), or with mixtures of acetone and other known ketonic solvents such as methyl ethyl ketone (MEK), diethyl ketone (DEK), methyl propyl ketone (MPK), and methyl iso-butyl ketone (MIBK), cyclohexanone, and (2) thermoplastic PVC or CPVC resins. Primers are also provided in accordance with the present invention by omitting the inclusion of the thermoplastic resin.
- DMPD low vapor pressure isomeric dimethyl-2-piperidones
- the novel adhesives described herein overcome the deficiencies described above for the prior art adhesives without compromising adhesive performance.
- the adhesives of the present invention comprise (for joining PVC pipes and components):
- the foregoing composition is modified only by replacing the resin component in (a) with about 5 to 25 wt % CPVC resin.
- DMPD which is used in the novel adhesive of the present invention, is a true solvent for PVC and CPVC and exhibits a remarkable decrease in solution viscosity when blended with the non-solvent acetone or the other ketones (such as methyl ethyl ketone, diethyl ketone, methyl propyl ketone, cyclohexanone, methyl iso-butyl ketone, methyl amyl ketone, acetophenone, methyl iso-propyl ketone, methyl butyl ketone, methyl iso-amyl ketone, di-butyl ketone, ethyl amyl ketone, etc.), thereby allowing great latitude in formulation.
- Blends of DMPD can be adjusted for such parameters as set time, VOC content, cost, viscosity, flash point, solids content very readily with little effect on adhesive performance.
- the adhesive in this invention may include filler, thixotropic agents, colorants, stabilizers, oligomeric and polymeric rheology additives, wetting agents and adhesion promoters.
- the blended mixture yields PVC or CPVC pipe adhesives that:
- VOC formulas e.g., less than 510 g/l for PVC pipe and less than 490 g/l for CPVC pipe
- (5) can be formulated with minimal (10 wt % maximum) or no cyclic ethers such as THF.
- novel low VOC solvent-based adhesives comprising a mixture of low vapor pressure isomeric dimethyl-2-piperidones (DMPD) blended with (1) (a) a non-solvent diluent, specifically, acetone (a VOC-exempt compound), or (b) with mixtures of acetone and other known ketonic solvents such as methyl ethyl ketone (MEK), diethyl ketone (DEK), methyl propyl ketone (MPK), methyl iso-butyl ketone (MIBK), methyl amyl ketone (MAK), and cyclohexanone, or (c) with one or more of the foregoing ketonic solvents without acetone, and (2) thermoplastic PVC or CPVC resins.
- DMPD low vapor pressure isomeric dimethyl-2-piperidones
- the novel adhesives described herein overcome the deficiencies described above for the prior art adhesives without compromising adhesive performance.
- the adhesives of the present invention comprise (for joining PVC pipes and components):
- the foregoing composition is modified only by replacing the resin component in (a) with about 5 to 25 wt % CPVC resin.
- the concentration of a particular component is with respect to the total adhesive or primer composition.
- the purity of all components is that employed in normal commercial practice in the field of PVC and CPVC adhesives and primers for joining pipes and other components together.
- DMPD which is used in the novel adhesive of the present invention, is a true solvent for PVC and CPVC and exhibits a remarkable decrease in solution viscosity when blended with the non-solvent acetone or the other ketones (such as methyl ethyl ketone, diethyl ketone, methyl propyl ketone, cyclohexanone, methyl iso-butyl ketone, methyl amyl ketone, acetophenone, methyl iso-propyl ketone, methyl butyl ketone, methyl iso-amyl ketone, di-butyl ketone, ethyl amyl ketone, etc.), thereby allowing great latitude in formulation.
- the non-solvent acetone or the other ketones such as methyl ethyl ketone, diethyl ketone, methyl propyl ketone, cyclohexanone, methyl iso-butyl ketone,
- Blends of DMPD can be adjusted for such parameters as set time, VOC content, cost, viscosity, flash point, solids content very readily with little effect on adhesive performance.
- isomers of DMPD including 1,3-dimethyl piperidone, 1,4-dimethyl piperidone, 1,5-dimethyl piperidone, 2,3-dimethyl piperidone, 2,4-dimethyl piperidone, and 2,5-dimethyl piperidone, all of which alone or in any combination are useful in the practice of the present invention.
- One product that is commercially available comprises a mixture containing 64 to 71 wt % of 1,3-dimethyl piperidone and 29 to 36 wt % of 1,5-dimethyl piperidone and is available from E. I. du Pont de Nemours (Wilmington, Del.).
- acetone may be employed as the sole ketone in the range of about 15 to 75 wt % of the total adhesive or primer composition.
- a mixture of acetone and at least one of the other above-enumerated ketones may be employed, the total concentration falling within the same range.
- at least one of the enumerated ketones, other than acetone may be used in the practice of the present invention.
- the ketone component comprises about 10 to 75 wt % of the total adhesive or primer composition and is at least one ketone selected from the group consisting of (1) 0 to about 75 wt % acetone; (2) 0 to about 75 wt % of at least one low boiling ketone having a boiling point less than 80° C., such as methyl ethyl ketone (MEK); (3) 0 to 35 wt % of at least one medium boiling ketone having a boiling point within a range of about 80° to 130° C., such as diethyl ketone (DEK), methyl propyl ketone (MPK), methyl iso-propyl ketone (MIPK), methyl iso-butyl ketone (MIBK), and methyl n-butyl ketone (MBK); and (4) 0 to about 35 wt % of at least one high boiling ketone having a boiling point greater than 130° C., such as cyclohexan
- acrylic resin With regard to the PVC resin, its incorporation into the adhesive composition provides an adhesive for PVC pipe.
- acrylic resins may be included, as disclosed in U.S. Pat. No. 5,422,388, issued to Naresh D. Patel et al on Jun. 6, 1995.
- the acrylic resin if employed, may comprise any combination of the known homopolymers, copolymers, and terpolymers commonly employed in adhesive compositions.
- the concentration of PVC resin is in the range of about 5 to 25 wt % of the total adhesive composition.
- the acrylic resin if employed, is preferably in the range of about 2 to 25 wt %, with the concentration of the mixture of both PVC and acrylic resin ranging from about 10 to 35 wt % of the adhesive composition. (A minimum of 10 wt % resin is permitted under ASTM-2564.) A concentration of PVC beyond the maximum value of 25 wt % would not be shelf-stable. With regard to the acrylic resin, less than about 2 wt % does not result in the benefits provided to the adhesive by its presence in combination with the PVC resin, while greater than about 25 wt % is not soluble in the solvent system. Within the foregoing constraints, the total resin level in the PVC adhesive ranges from about 10 to 35 wt %, as indicated above.
- PVC resins commonly employed in PVC adhesives may be used in the practice of the present invention.
- Particularly preferred are those PVC resins characterized by homopolymers as classified by inherent viscosity (I.V.) in the range of about 0.6 to 0.95.
- the inherent viscosity of a PVC resin is determined in accordance with ASTM D-1243. Inherent viscosity is a qualitative measure of molecular weight; that is, the higher the I.V., the higher the molecular weight.
- a non-limiting example of a suitable PVC resin employed in the practice of the present invention is Shintech SE-650, available from Shintech, Inc. (Freeport, Tex.).
- the acrylic resins advantageously employed in the practice of the present invention are those homopolymers, copolymers, and terpolymers of methyl methacrylate.
- the useful range in the practice of the present invention is 0.1 to 1.25.
- an acrylic resin having a melt flow rate as determined by ASTM D-1238 in the range of 1.6 to 24 is acceptable.
- the CPVC resin With regard to the CPVC resin, its incorporation into the adhesive composition provides an adhesive for CPVC pipe. As indicated above, the CPVC resin is contained in the adhesive formulation in an amount ranging from about 5 to 25 wt %, preferably from about 5 to about 15 wt % of the total adhesive. If too small an amount of CPVC resin is used, it may not be possible to form an effective and durable pipe joint and VOC levels will tend to increase, while, if the amount of CPVC resin too great, it may not all solubilize in the solvent(s) and thus tends to form an undesirable āgelā therewith.
- CPVC resins useful in this invention may be prepared by chlorination of polyvinyl chloride homopolymers and copolymers starting materials by procedures known to those skilled in the art. Examples of useful polyvinyl chloride homopolymers and copolymers starting materials in this regard include those described in U.S. Pat. No. 5,384,345, which teachings are incorporated herein by reference.
- CPVC resins are typically supplied in powder form when obtained from commercial sources.
- the CPVC resins used in this invention may contain chlorine in any amount effective to impart adequate heat deflection resistance property to the adhesive composition for the intended use(s).
- the chlorine content of the CPVC resins used in the compositions of this invention will range from about 50 to about 80% by weight, and more specifically about 57 to about 70% by weight.
- CPVC resins characterized by an inherent viscosity (I.V.) ranging from about 0.60 to 0.95, and more preferably about 0.68 to about 0.92.
- I.V. inherent viscosity
- a non-limiting example of a suitable CPVC resin employed in the practice of the present invention is BF Goodrich Temprite 677 ā 670 with 67% chlorination, available from BF Goodrich (Cleveland, Ohio).
- the adhesives of the present invention may include additional solids.
- additional solids that may be present include fillers, thixotropic agents, colorants, stabilizers, oligomeric and polymeric rheology additives, wetting agents, and adhesion promoters. Up to about 8 wt % of the adhesive may contain such additional additives and adjuvants. Any fillers, thixotropic agents, pigments, dyes, stabilizers oligomeric and polymeric rheology additives, wetting agents, and adhesion promoters that are commonly used in PVC and CPVC adhesives may be employed in the practice of the present invention.
- Preferred fillers low specific gravity hollow spheres glass, ceramic, or synthetic, e.g., PVC
- PVC polyvinyl styrene
- solid particulate inorganic fillers such as calcium carbonate, aluminum trihydrate, calcium sulfate, and crystalline silica.
- Preferred colorants include dyes and pigments, such as titanium dioxide, carbon black, aluminum Lake based-orange, and conventional red or yellow colorants.
- Preferred thixotropic agents include fumed silica and precipitated silica (e.g., AEROSIL-200 available from Degussa Corporation, Cab-O-Sil MS available from Cabot Corporation, and HISIL T600) and treated bentonite clay (e.g., Bentone 27), and these may be used at low levels to obtain optimum flow properties, especially with regard to controlling spillage from the pipe upon application.
- fumed silica and precipitated silica e.g., AEROSIL-200 available from Degussa Corporation, Cab-O-Sil MS available from Cabot Corporation, and HISIL T600
- bentonite clay e.g., Bentone 27
- Preferred stabilizers include such additives as acid scavengers, antioxidants (e.g., hindered phenols) and tin stabilizers.
- Preferred rheology additives include non-PVC or non-CPVC thermoplastic resins, such as one or more of thermoplastic PVC polymers (in the case of CPVC adhesives), acrylic polymers (in the case of CPVC adhesives), MBS polymers, ABS polymers, linear and core/shell polymers, and random and block polymers including elastomeric and rubber resins.
- the blended mixture yields PVC or CPVC pipe adhesives that:
- VOC formulas e.g., less than 510 g/l for PVC pipe and less than 490 g/l for CPVC pipe
- (5) can be formulated with minimal (10 wt % maximum) or no (0 wt %) cyclic ethers such as THF.
- composition ranges are preferred. These include:
- cyclohexanone up to about 35 wt % cyclohexanone, where acetone and cyclohexanone together total about 10 to 68 wt % of the adhesive.
- cyclohexanone up to about 35% of at least one of cyclohexanone, MPK, and DEK, where acetone, MPK, DEK, and cyclohexanone together total about 10 to 68 wt % of the adhesive.
- cyclohexanone up to about 35 wt % cyclohexanone, wherein methyl ethyl ketone, MPK, DEK, and cyclohexanone together total about 10 to 68 wt % of the adhesive.
- the PVC or CPVC resin may have a concentration as low as 5 wt %. Such a formulation is still an adhesive, but it falls below the minimum of 10 wt % required to satisfy ASTM compliance.
- the primer for joining PVC pipes and components or CPVC pipes and components comprises:
- compositions listed in Table I below exemplify some typical preferred compositions with low VOC values.
- SCAQMD Rule 1168 specifies a VOC level for PVC adhesives of 510 g/l or less.
- DMND and MEK adhesives result in acceptable VOC levels; in Examples 4-6, the DMPD and acetone formulas evidence much lower VOC levels as a result of acetone being an exempt compound.
- Comparative Examples 1 and 2 in Table II show VOC levels exceeding 500 g/l for a typical THF/resin adhesive (Comparative Example 1) and for a typical commercial cement Weld-On 711 (Comparative Example 2).
- Examples 1-6 in Table I also exemplify the low values of these DMPD base adhesives, which are commercially desirable, since they can be readily increased using thixotropic agents such as fumed silica or rheology additives such as homo-, co-, or ter-polymeric methacrylate, MBS (methyl methacrylate-butadiene-styrene), ABS (acrylonitrile-butadiene-stryene), etc. to give desirable flow characteristics and body to the adhesives.
- thixotropic agents such as fumed silica or rheology additives
- MBS methyl methacrylate-butadiene-styrene
- ABS acrylonitrile-butadiene-stryene
- compositions listed in Table III exemplify the wide latitude in formulation with based adhesives with respect to adhesive performance.
- Formulas of DMPD with acetone (Examples 7, 8, 11, 13); DMPD with acetone, MEK, and cyclohexanone (Example 9); DMPD with MEK and cyclohexanone (Example 12); and DMPD and MEK (Example 15) all satisfy the minimum lap shear values for 2, 16, and 72 hours as required in ASTM D-2564 for PVC.
- Examples 7-15 clearly demonstrate to one skilled in the art that various changes and modifications may be used to adjust set-time, viscosity, VOC levels, bond strength and formulations costs and such changes and modifications are considered to fall within the scope of the invention.
- these DMPD formulations can be made to include other known PVC and CPVC solvents such as THF, NMP, aliphatic and aromatic ketones to further adjust desired adhesive properties.
- formulation comprising various molecular weight thermoplastic PVC and CPVC with DMPD blends would be obvious to one skilled in the art as exemplified in Example 13.
- Table IV lists the solution properties of adhesives containing PVC resins having I.V. values ranging from 0.68 to 0.90.
- Table IV illustrates that DMPD readily dissolves various PVC resins (of different I.V.) to give 10 wt % solutions with low viscosities. This is meant to show that cements can be formulated with a range of PVC molecular weights (based on I.V. value). While the DMPD concentration is higher than discussed earlier, it is listed here to show that although such compositions are very slow drying, nevertheless, the compositions are still good adhesives.
- ASTM F-656 requires that a solvent/solvent blend is a primer if it can dissolve 10 wt % resin.
- Table V lists the hydrostatic burst strength of adhesives containing CPVC resins.
- the hydrostatic burst strengths were measured in accordance with ASTM-F493.
- Table V lists some specific examples of CPVC low VOC cement formulations containing DMPD, MEK, and acetone. These formulations show the solvency of DMPD/MEK/acetone combinations and their effectiveness as CPVC cements. It would be obvious to one skilled in this art that other solvent blends of DMPD/MEK/acetone and other ketones such as DEK, cyclohexanone, etc., as well as formulas with minimal amounts of THF, lend themselves as cements for CPVC articles such as pipes, fittings, etc.
- the adhesives and primers disclosed herein are expected to find use in joining PVC and CPVC pipes and other such articles together.
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Abstract
Description
TABLE I |
Compositions and Results for Examples 1-6. |
Ingredients | 1 | 2 | 3 | 4 | 5 | 6 |
MEK | ā | 44.00 | 66.00 | ā | ā | 24.00 |
Cyclohexanone | ā | ā | ā | ā | ā | 15.00 |
Acetone | ā | ā | ā | 44.00 | 66.00 | 24.00 |
Dimethyl piperidone | 90.00 | 44.00 | 22.00 | 44.00 | 22.00 | 25.00 |
SE-650 PVC resin (I.V. = 0.68) | 10.00 | 12.00 | 12.00 | 12.00 | 12.00 | 12.00 |
Total | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 |
Viscosity (cps) | 175 | 70 | 60 | 60 | 120 | 60 |
Spindle/Speed | 2@60 | 2@60 | 2@60 | 2@60 | 2@60 | 2@60 |
Specific Gravity | 1.024 | 0.937 | 0.891 | 0.931 | 0.883 | 0.916 |
VOC/SCAQMD method# | 235 | 461 | 483 | 298 | 197 | 375 |
316-A (Rev 04/95) (max: 510 g/l) | ||||||
Hydrostatic Burst Strength per | Passed | Passed | Passed | Passed | Passed | |
ASTM D-2564 (min. req'd: 400 | ||||||
psi) | ||||||
TABLE II |
Compositions and VOC and Lap Shear Strength for |
Comparative Examples 1 and 2. |
Comparative Ex- | Comparative Ex- | |
Ingredients | ample 1 | ample 2 |
THF | 80.50 | A typical |
Cyclohexanone | ā | PVC |
Cyclohexanone | ā | cement, |
Acetone | ā | Weld-On#711 |
Dimethyl piperidone | ā | ā |
SE-650 PVC resin (I.V. = 0.68) | 19.50 | PVC |
Total | 100.00ā | |
Viscosity (cps) | 500 | |
Spindle/Speed | 2@30 | |
VOC/SCAQMD method# | 528 | 600 |
316-A(Rev 04/95) |
Lap Shear Strength | Avg | 288 | Pass |
per ASTM D-2564 | |||
Time: 2 hrs. | |||
Min. Req'd: 250 psi | |||
Lap Shear Strength | Avg | 673 | Pass |
per ASTM D-2564 | |||
Time: 16 hrs. | |||
Min. Req'd: 500 psi | |||
Lap Shear Strength | Avg | 1391ā | Pass |
per ASTM D-2564 | |||
Time: 72 hrs. | |||
Min. Req'd: 900 psi | |||
TABLE III |
Compositions and Lap Shear Strength/ASTM-D2564 for Examples 7-15. |
Ingredients | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 |
MEK | ā | ā | 23.50 | ā | ā | 47.00 | ā | ā | 60.00 |
Cyclohexanone | ā | ā | 15.00 | 15.00 | ā | 15.00 | ā | ā | ā |
Acetone | 68.00 | 45.00 | 23.50 | 47.00 | 60.00 | ā | 45.00 | 43.50 | ā |
Dimethyl Piperidone | 22.00 | 45.00 | 25.00 | 25.00 | 30.00 | 25.00 | 45.00 | 43.50 | 30.00 |
SE-650 PVC resin | 10.00 | 10.00 | 13.00 | 13.00 | 10.00 | 13.00 | ā | 13.00 | 10.00 |
(I.V. = 0.68) | |||||||||
SE-950 PVC resin | ā | ā | ā | ā | ā | ā | 10.00 | ā | ā |
(I.V. = 0.92) | |||||||||
Total | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 |
Viscosity (cps) | 75 | 40 | 95 | 90 | 35 | 95 | 120 | 90 | 45 |
Spindle/Speed | 2@60 | 2@60 | 2@60 | 2@60 | 2@60 | 2@60 | 2@60 | 2@60 | 2@60 |
C.S. Strength | Avg | 358 | 308 | 286 | 297 | 311 | 269 | 289 | 334 | 350 |
Time: 2 Hrs. | ||||||||||
Substrate: PVC | ||||||||||
Wipe W/:MEK | ||||||||||
C.S. Strength | Avg | 846 | 661 | 603 | 576 | 573 | 503 | 558 | 566 | 632 |
Time: 16 Hrs. | ||||||||||
Substrate: PVC | ||||||||||
Wipe W/: MEK | ||||||||||
C.S. Strength | Avg | 1480 | 1178 | 975 | 913 | 1355 | 925 | 949 | 1029 | 1148 |
Time: 72 Hrs. | ||||||||||
Substrate: PVC | ||||||||||
Wipe W/: MEK | ||||||||||
Hydrostatic Burst | Passed | Passed | Passed | Passed | Passed | Passed | Passed | Passed | Passed | |
Strength per ASTM | ||||||||||
D-2364 (min. req'd: | ||||||||||
400 psi | ||||||||||
TABLE IV |
Compositions and Results for Examples 16-19. |
16 | 17 | 18 | 19 | ||
Dimethyl piperidone | 90.00 | 90.00 | 90.00 | 90.00 |
SE-650 PVC resin (I.V. = 0.68) | 10.00 | ā | ā | ā |
SE-750 PVC resin (I.V. = 0.74) | ā | 10.00 | ā | ā |
SE-800 PVC resin (I.V. = 0.78) | ā | ā | 10.00 | ā |
SE-950 PVC resin (I.V. = 0.90) | ā | ā | ā | 10.00 |
Total | 100.00 | 100.00 | 100.00 | 100.00 |
Viscosity (cps) | 175 | 225 | 255 | 405 |
Spindle/Speed | 2@60 | 2@60 | 2@60 | 2@60 |
Specific Gravity | 1.024 | 1.024 | 1.025 | 1.025 |
TABLE V |
Compositions and Results for Examples 20-23. |
20 | 21 | 22 | 23 | ||
MEK | 60.00 | 43.00 | ā | ā |
Acetone | ā | ā | 60.00 | 43.00 |
Dimethyl piperidone | 26.00 | 43.00 | 26.00 | 43.00 |
BFG - 677x670 CPVC resin | 14.00 | 14.00 | 14.00 | 14.00 |
Total | 100.00 | 100.00 | 100.00 | 100.00 |
Viscosity (cps) | 175 | 225 | 255 | 405 |
Spindle/Speed | 2@60 | 2@60 | 2@60 | 2@60 |
Specific Gravity | 1.024 | 1.024 | 1.025 | 1.025 |
Hydrostatic Burst | 1 | 550 | 400 | 450 | 425 |
Pressure per ASTM | 2 | 550 | 425 | 425 | 400 |
F-493 | 3 | 550 | 400 | ||
Test Temp.: R.T. | Avg. | 550 | 408 | 438 | 413 |
Min. Req'd: 400 psi | |||||
Hydrostatic Burst | 1 | 360 | 310 | 300 | 310 |
Pressure per ASTM | 2 | 340 | 350 | 310 | 290 |
F-493 | 3 | 310 | 290 | 290 | |
Test Temp.: 180° F. | Avg. | 350 | 323 | 300 | 297 |
water | |||||
Min. Req'd: 200 psi | |||||
Claims (25)
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US09/651,824 US6372821B1 (en) | 1999-02-23 | 2000-08-30 | Low VOC (volatile organic compounds), dimethyl-2-piperidone solvent-based, PVC and CPVC pipe and component adhesives and primers containing minimal or no tetrahydrofuran |
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US20040063826A1 (en) * | 2002-09-30 | 2004-04-01 | Sobieski Robert T. | Halogen-containing vinyl polymer compounds |
US20040061095A1 (en) * | 2002-09-30 | 2004-04-01 | Sobieski Robert T. | Halogen-containing vinyl polymer stabilizers |
US7029759B2 (en) | 2002-09-30 | 2006-04-18 | Omnova Solutions Inc. | Halogen-containing vinyl polymer compositions |
US20040063822A1 (en) * | 2002-09-30 | 2004-04-01 | Sobieski Robert T. | Halogen-containing vinyl polymer compositions |
US20060252865A1 (en) * | 2005-05-06 | 2006-11-09 | Bush Charles N | Universal solvent cement |
US7592385B2 (en) | 2005-05-06 | 2009-09-22 | Oatey Company | Universal solvent cement |
US7648603B2 (en) | 2006-08-02 | 2010-01-19 | Hercules Chemical Company Incorporated | Colorless primer composition and method |
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US7838585B2 (en) | 2008-07-11 | 2010-11-23 | Oatey Company | Plastic adhesive |
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US9611409B2 (en) | 2010-08-23 | 2017-04-04 | Oatey Co. | Color developing colorless primer |
US20160115358A1 (en) * | 2014-10-23 | 2016-04-28 | Ips, Corporation -Weld-On Division | Solvent cement for bonding thermoplastic resin articles |
US11674060B2 (en) | 2016-02-05 | 2023-06-13 | Oatey Co. | Solvent cement formulations |
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US12129405B2 (en) | 2016-02-05 | 2024-10-29 | Oatey Co. | Solvent cement formulations |
WO2018153825A1 (en) * | 2017-02-23 | 2018-08-30 | Henkel Ag & Co. Kgaa | Adhesive composition for bonding shaped parts made of plastic |
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CN109385232A (en) * | 2018-10-30 | 2019-02-26 | ę±čäŗæč¶ å·„ēØå”ęęéå ¬åø | A kind of PVC pipeline Adhesive for Sealing Steel Drum and preparation method thereof |
US11597859B2 (en) | 2020-01-24 | 2023-03-07 | Oatey Co. | Solvent cement formulations having extended shelf life |
US11976222B2 (en) | 2020-01-24 | 2024-05-07 | Oatey Co. | Solvent cement formulations having extended shelf life |
WO2024018482A1 (en) * | 2022-07-18 | 2024-01-25 | Ashirvad Pipes Pvt Ltd | A low voc solvent cement formulation with reduced toxicity and rapid curing |
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